Canonical Allele Identifier: PA2826558252
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6900
ClinVar RCV Id: RCV000007309 RCV000155750 RCV000221353 RCV002228004 RCV001810833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Met66Val
CA016797
NM_001276503.2:c.196A>G